Stability kinetics of ginsenosides in aqueous solution. 1984

E Miyamoto, and S Odashima, and I Kitagawa, and A Tsuji

The stability of ginsenosides (Rb1, Rb2, and Rg1) in aqueous solutions of varying pH was studied kinetically at 37 degrees C and an ionic strength of 0.15, using reverse-phase high-performance liquid chromatography. Degradation readily occurred by a proton-catalyzed reaction, the half-lives being only approximately 30 min at pH 1. However, under neutral intestinal pH conditions, the degradation was almost negligible throughout the experimental period (approximately 40 h).

UI MeSH Term Description Entries
D007700 Kinetics The rate dynamics in chemical or physical systems.
D004355 Drug Stability The chemical and physical integrity of a pharmaceutical product. Drug Shelf Life,Drugs Shelf Lives,Shelf Life, Drugs,Drug Stabilities,Drugs Shelf Life,Drugs Shelf Live,Life, Drugs Shelf,Shelf Life, Drug,Shelf Live, Drugs,Shelf Lives, Drugs
D006863 Hydrogen-Ion Concentration The normality of a solution with respect to HYDROGEN ions; H+. It is related to acidity measurements in most cases by pH pH,Concentration, Hydrogen-Ion,Concentrations, Hydrogen-Ion,Hydrogen Ion Concentration,Hydrogen-Ion Concentrations
D006868 Hydrolysis The process of cleaving a chemical compound by the addition of a molecule of water.
D012503 Saponins A type of glycoside widely distributed in plants. Each consists of a sapogenin as the aglycone moiety, and a sugar. The sapogenin may be a steroid or a triterpene and the sugar may be glucose, galactose, a pentose, or a methylpentose. Saponin
D012996 Solutions The homogeneous mixtures formed by the mixing of a solid, liquid, or gaseous substance (solute) with a liquid (the solvent), from which the dissolved substances can be recovered by physical processes. (From Grant & Hackh's Chemical Dictionary, 5th ed) Solution
D036145 Ginsenosides Dammarane type triterpene saponins based mainly on the aglycones, protopanaxadiol and protopanaxatriol. Ginsenoside,Panaxosides,Sanchinosides

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